A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609066



Internal ID20982137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166640539..167163432hg38UCSC Ensembl
chr6:167054027..167576920hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38522894
hg19522894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217037
Samples
Known GenesCCR6, FGFR1OP, GPR31, MIR3939, RNASET2, RPS6KA2, RPS6KA2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609066
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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